A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110192



Internal ID18930428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1884570..1886270hg38UCSC Ensembl
Outerchr11:1905800..1907500hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959459
SamplesKWS1
Known GenesLSP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110192
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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